diniconazole and penconazole

diniconazole has been researched along with penconazole* in 2 studies

Other Studies

2 other study(ies) available for diniconazole and penconazole

ArticleYear
Polyethylene glycol grafted flower-like cupric nano oxide for the hollow-fiber solid-phase microextraction of hexaconazole, penconazole, and diniconazole in vegetable samples.
    Journal of separation science, 2016, Volume: 39, Issue:16

    A simple, rapid, highly efficient, and reliable sample preparation method has been developed for the extraction and analysis of triazole pesticides from cucumber, lettuce, bell pepper, cabbage, and tomato samples. This new sorbent in the hollow-fiber solid-phase microextraction method is based on the synthesis of polyethylene glycol-polyethylene glycol grafted flower-like cupric oxide nanoparticles using sol-gel technology. Afterward, the analytes were analyzed by high-performance liquid chromatography with ultraviolet detection. The main parameters that affect microextraction efficiency were evaluated and optimized. This method has afforded good linearity ranges (0.5-50 000 ng/mL for hexaconazol, 0.012-50 000 ng/mL for penconazol, and 0.02-50 000 ng/mL for diniconazol), adequate precision (2.9-6.17%, n = 3), batch-to-batch reproducibility (4.33-8.12%), and low instrumental LODs between 0.003 and 0.097 ng/mL (n = 8). Recoveries and enrichment factors were 85.46-97.47 and 751-1312%, respectively.

    Topics: Chromatography, High Pressure Liquid; Copper; Food Contamination; Limit of Detection; Pesticides; Polyethylene Glycols; Solid Phase Microextraction; Triazoles; Vegetables

2016
Enantiomeric separation of triazole fungicides with 3-μm and 5-μml particle chiral columns by reverse-phase high-performance liquid chromatography.
    Chirality, 2011, Volume: 23, Issue:6

    This study used chiral columns packed with 3-μm and 5-μm particles to comparatively separate enantiomers of 9 triazole fungicides, and Lux Cellulose-1 columns with chiral stationary phase of cellulose-tris-(3,5-dimethylphenylcarbamate) were used on reverse-phase high-performance liquid chromatography with flow rates of 0.3 and 1.0 mL min(-1) for 3-μm and 5-μm columns, respectively. The (+)-enantiomers of hexaconazole (1), tetraconazole (4), myclobutanil (7), fenbuconazole (8) and the (-)-enantiomers of flutriafol (2), diniconazole (3), epoxiconazole (5), penconazole (6), triadimefon (9) were firstly eluted from both columns, the elution orders identified with an optical rotation detector didn't change with variety of column particles and mobile phases (acetronitrile/water and methanol/water). The plots of natural logarithms of the selectivity factors (ln α) for all fungicides except penconazole (6) versus the inverse of temperature (1/T) were linear in range of 5-40°C. The thermodynamic parameters (ΔH°, ΔS°, ΔΔH° and ΔΔS°) were calculated using Van't Hoff equations to understand the thermosynamic driving forces for enantioseparation. This work will be very helpful to obtain good enantiomeric separation and establish more efficient analytical method for triazole fungicides. Chirality, 2011. © 2011 Wiley-Liss, Inc.

    Topics: Animals; Chlorobenzenes; Chromatography, High Pressure Liquid; Chromatography, Reverse-Phase; Epoxy Compounds; Fungicides, Industrial; Mice; Nitriles; Particle Size; Stereoisomerism; Temperature; Thermodynamics; Triazoles

2011